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Reproductive Patterns of Bogue, Boops Boops (Sparidae), in the Southeastern Adriatic Sea

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Reproductive Patterns of Bogue, Boops Boops (Sparidae), in the Southeastern Adriatic Sea ISSN: 0001-5113 ACTA ADRIAT., ORIGINAL SCIENTIFIC PAPER AADRAY 58(1): 117 - 125, 2017 Reproductive patterns of bogue, Boops boops (Sparidae), in the southeastern Adriatic Sea Tatjana DOBROSLAVIĆ*, Renata MOZARA, Branko GLAMUZINA and Vlasta BARTULOVIĆ University of Dubrovnik, Department of Aquaculture, Ćira Carića 4, Croatia *Corresponding author, e-mail: [email protected] The reproductive characteristics of bogue (Boops boops) in the southeastern Adriatic Sea are presented in this study. The analysis is based on 676 specimens caught by seine net from December 2011 to November 2012. Total length of females ranged from 13.3 to 29.3 cm and males from 15.1 to 26.3 cm. The overall sex ratio of females to males was 1:0.85 (χ2=4.314; P < 0.05) with a slightly higher number of females in the largest size class. Length-weight relationship for the total population indicated negative allometric growth (b=2.911). Values of the condition factor are relatively low for both sexes. Maximum values were recorded in September 1.025 for females and 1.029 for males. Gonadosomatic index and histological examination showed that the spawning season of the bogue in the Adriatic is from January to May with peak in February. Six stages of gonad development were identified: immature, undergoing maturation, ripening, ripe, spawning and spent. The monthly distribution of the different sexual maturity stages and the frequency distribution of oocyte diameter revealed that this species is a batch spawner. Key words: length-weight relationship, oogenesis, spermatogenesis, reproduction, Boops boops INTRODUCTION 1996; RELINI et al., 1999). Females of bogue reach sexual maturity at length of 12 cm and males at The bogue, Boops boops (Linnaeus, 1758) 13 cm (JARDAS, 1996; EL-AGAMY et al., 2004). Her- is one of the most abundant species of the fam- maphroditic behaviour has been reported in this ily Sparidae (NELSON, 2006). It mainly inhabits species in the basic form of protoginy. Males Mediterranean Sea and eastern Atlantic (JARDAS, may develop directly from the juvenile state or 1996). It is the only Sparidae species included in may develop from adult females by sex change the top 13 most landed demersal fish species in (GORDO, 1995). the Mediterranean Sea, despite its low commer- Despite the fact that it is commercially cial value (LLEONART & MAYNOU, 2003). important species in the Adriatic Sea only some The bogue is a medium sized, up to 36.0 aspects such as, length-weight relationship cm total length, more common between 10.0 (DULČIĆ & GLAMUZINA, 2006) and juveniles diet and 20.0 cm, demersal and semipelagic species (DOBROSLAVIĆ et al., 2012) have been investi- (JARDAS, 1996). It can be found as deep as 350 gated. Reproductive biology of this species was m over a variety of substrates including mud, studied in the Aegean Sea (SOYKAN et al., 2015), sand, rocks and seaweeds, though it is more Tyrrhenian Sea (BOTTARI et al., 2014), Egyptian abundant at depths of 100 m and less (JARDAS, coast of Mediterranean (EL-AGAMY et al., 2004) 118 ACTA ADRIATICA, 58(1): 117 - 124, 2017 and on the Portuguese coast (GORDO, 1995; MON- classifies as: oocytes in primary growth (early TEIRO et al., 2006). and advanced), cortical alveoli stage, vitello- The aim of this study was to describe repro- genesis (early and advanced), migratory nucleus ductive characteristics of bogue in the Adriatic stage, hydrated oocytes and postovulatory fol- Sea, based on histological analysis of gonad licles (HUNTER et al., 1986; TYLER & SUMPTERN, development. Due to the fact that all aspects of 1996). Male germ cells were classified as: sper- reproductive biology have an important role for matogonia, spermatocysts, spermatids and sper- assessment and management plans as well as matozoa (GRIER, 1981). understanding annual changes in the population, Gravimetric method was used to estimate data obtain in this study can be used for future total fecundity. For each female (n=60) after stock management of this species. weighing the ovaries, three (F1, F2, F3) subsam- ples (0,001 g) were taken from anterior, central MATERIAL AND METHODS and posterior ovary lobe. The number of eggs in each subsample was estimated using the follow- Adult specimens were collected monthly ing equation: Fecundity = Number of eggs in from December 2011 to November 2012 in the subsample x Ovary weight / Weight of subsam- southern Adriatic Sea (42.75°N; 17.83°E) using ple. The individual fecundity for each female seine net. A total of 676 individuals were exam- was calculated by following equation Fecun- ined in this study period. For each fish, total dity = F1+F2+F3/3 (LAEVASTU, 1965, YELDEN & length (TL) was measured to the nearest 0.1 cm AVSAR, 2000). and weighed (W) to the nearest 0.1 g. Fish was gutted, and gonads were removed and weight RESULTS AND DISCUSSION (±0.001) measured. The length-weight relation- ship was determined by linear regression analy- Out of 676 individuals, 365 (50.7%) were sis and scatter diagrams of length and weight females and 311 (43.2%) males. Total length were plotted. It was calculated using equation of females ranged from 13.3 to 29.3 cm with a W=aLb; where a is the regression intercept and mean value of 18.41 ± 2.0 cm and males from b is the regression slope, W is the wet weight 15.1 to 26.3 cm (18.29 ± 1.72 cm) (Fig. 1) with (g) and L is the total length (cm) (FROESE, 2006). no statistically significant difference between Fultonʼs condition factor was calculated follow- females and males (Mann-Whitney U= 54493, ing FROESE (2006): K=(W/L3)×100. P>0,05). The overall sex ratio of females to 2 Spawning period was established with males was 1:0.85 (χ =4.314; P < 0.05). monthly variations of the gonadosomatic index Length-weight relationship shows negative 2.884 allometric growth for females (W=0.0131 Lt , (GSI) calculated as: GSI= (Wg/(W–Wg))×100, where Wg is gonad and Wt total body weight. For histological analysis gonad tissue of 120 females and 120 males was fixed in 8% buffered forma- lin. Fixation was followed by dehydration in increasingly concentrated ethanol, tissue clear- ing and embedding in paraffin. Tissue was then sectioned on microtome (5 µm) and stained by hematoxylin and eosine dye. After the standard tissue processing histological slides were used for defining the gonads development stages. It was classified following the classification pro- MURUA & MOTOS (2006) posed by as: immature, Fig.1. Length frequency distribution of male (n=311) and undergoing maturation, ripening, ripe, spawning female (n=365) bogue, Boops boops in the Adriatic or spent. Stages of oocyte development were Sea Dobroslavić et al.:Reproductive patterns of bogue, Boops boops (Sparidae), in the Adriatic Sea ... 119 Table 1. Comparison of the values of weight-length relationships for Boops boops obtained in this study with other stud- ies carried out in the Adriatic Sea, Portugal coast, SW Spain, Tyrrhenian and Aegean Sea (LR – length range; GT – growth type) Authors Location n LR (cm) a b R2 GT Gonçalves et al. (1997) SW Portugal coast 603 15.8-35.5 0.0758 3.037 0.91 +A Santos et al. (2002) South Portugal coast 90 14.2-28.2 0.0085 3.040 0.967 +A Monteiro et al. (2006) South Portugal coast 837 7.4-30.5 0.079 3.01 0.979 +A Dulčić & Glamuzina (2006) Eastern Adriatic Sea 85 9.7-16.7 0.0169 2.815 0.975 -A Torres et al. (2012) SW Spain 454 8.5-30.9 0.0147 2.842 0.94 -A Bottari et al. (2014) Tyrrhenian Sea 2217 23.0-33.0 0.023 3.118 0.995 +A Soykan et al. (2015) Aegean Sea 421 11.0-23.8 0.005 3.251 0.968 +A Present study Southern Adriatic Sea 720 13.3-29.3 0.0385 2.522 0.905 -A 2 2.963 2 R =0.907), males (W=0.0106 Lt , R =0.884) females and 0.85 for males. Monthly variation 2.911 and both sexes combined (W=0.0112 Lt , of condition factor shows a better condition R2=0.899). Changes in fish shape, growth incre- between May and October and decrease of the ment or break in growth, some of the environ- condition between December and April (Fig. 2). mental factors such as temperature and food Results from this study showed that values of availability can affect the growth exponent condition index follow the reproductive cycle (b) (FROST, 1945). Negative allometry was also with lower values recorded during the spawning recorded in other studies of length-weight rela- period of this species in the Adriatic Sea. The tionship in the Adriatic Sea (DULČIĆ & GLAMUZ- condition factor is a result of the weight-length INA, 2006) and in the study of TORRES et al. (2012) relationship and it is under direct influence of carried out at Gulf of Cadiz (SW Spain). In other age, sex, gonad maturity and fullness of the studies (GONÇALVES et al., 1997; SANTOS et al., stomach (BARNHAM & BAXTER, 1998). Condition 2002; MONTEIRO et al., 2006; BOTTARI et al., 2014; of the fish is also strongly influenced by biotic SOYKAN et al., 2015) growth of bogue showed environmental condition and can be used to positive allometry (Table 1). assess the ecosystem status (ANENE, 2005). Values of the condition factor are relatively Based on monthly obtained GSI values low for both sexes. Maximum values were spawning period of this species in the Adri- recorded in September 1.025 for females and atic Sea extend from January to May. Mean 1.029 for males and minimum in April 0.87 for maximum values were recorded in February Fig.
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